Merck
CN
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文件

安全信息

W248924

Sigma-Aldrich

糠醛

greener alternative

natural, ≥98%, FCC, FG

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别名:
2-呋喃醛, 呋喃-2-甲醛
经验公式（希尔记法）:
C5H4O2
CAS号:
98-01-1
分子量:
96.08
FEMA编号:
2489
Beilstein:
105755
EC 号:
202-627-7
MDL编号:
MFCD00003229
PubChem化学物质编号:
24900969
Flavis编号:
13.018

等级

FG
Fragrance grade
Halal
Kosher
natural

质量水平

400

Agency

follows IFRA guidelines
meets purity specifications of JECFA

管理合规性

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
FDA 21 CFR 175.105

蒸汽密度

3.31 (vs air)

蒸汽压

13.5 mmHg ( 55 °C)

检测方案

≥98%

形式

liquid

自燃温度

599 °F

expl. lim.

19.3 %

环保替代产品特性

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

折射率

n20/D 1.525 (lit.)

bp

162 °C (lit.)

mp

−36 °C (lit.)

溶解性

95% ethanol: soluble 1 mL/mL, clear

密度

1.16 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

致敏芳香化合物

no known allergens

环保替代产品分类

, Aligned

性状检查

almond; baked; bread; woody; sweet

SMILES字符串

[H]C(=O)c1ccco1

InChI

1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H

InChI key

HYBBIBNJHNGZAN-UHFFFAOYSA-N

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相关类别

一般描述

Furfural is a furan derivative. Production of furfural by dehydration of fructose, glucose and xylose using a biphasic reactor system has been reported. Furfural, a Maillard reaction product, is reported to inhibit the growth and alcohol production bySaccharomyces cerevisiae.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

警示用语：

Danger

危险分类

Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Aquatic Chronic 3 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

136.4 °F - closed cup

闪点(°C)

58 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品

分析证书(COA)

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Inhibition of glycolysis by furfural in Saccharomyces cerevisiae.
Banerjee N, et al.
Europ. J. Appl. Microbiol. Biotechnol., 11(4), 226-228 (1981)
Selective conversion of furfural to methylfuran over silica-supported Ni Fe bimetallic catalysts.
Sitthisa S, et al.
J. Catal., 284(1), 90-101 (2011)
Production of 5-hydroxymethylfurfural and furfural by dehydration of biomass-derived mono-and poly-saccharides.
Chheda JN, et al.
Green Chemistry, 9(4), 342-350 (2007)
Jianmin Zhang et al.
Journal of medicinal chemistry, 50(8), 1850-1864 (2007-03-27)
The 3C-like protease (3CLpro), which controls the severe acute respiratory syndrome (SARS) coronavirus replication, has been identified as a potential target for drug design in the treatment of SARS. A series of tetrapeptide phthalhydrazide ketones, pyridinyl esters, and their analogs
Selective hydrogenation of furfural and levulinic acid to biofuels on the ecofriendly Cu-Fe catalyst.
Yan K and Chen A.
Fuel: The Science and Technology of Fuel and Energy, 115, 101-108 (2014)
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